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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 500-88-9 Chemical Structure| 500-88-9

Structure of 500-88-9

Chemical Structure| 500-88-9

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Product Details of [ 500-88-9 ]

CAS No. :500-88-9
Formula : C9H13NO2
M.W : 167.21
SMILES Code : OC1=CC=C(CC(N)CO)C=C1
MDL No. :MFCD10034634

Safety of [ 500-88-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P260-P264-P280-P305+P351+P338-P405-P501
Class:8
UN#:3259
Packing Group:

Application In Synthesis of [ 500-88-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 500-88-9 ]

[ 500-88-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4089-07-0 ]
  • [ 500-88-9 ]
YieldReaction ConditionsOperation in experiment
54% With lithium aluminium tetrahydride; In diethyl ether; at 20℃; for 3h; Compound [2,] Tyrosinol To 3 gr, 12 mM, L-tyrosine ethyl [ESTER HCI] in 50 ml dry ether was added 1.2 gr 32 mM LiAIH4., After stirring 3 hours at room temperature, water and KOH were added and the reaction was extracted with ethyl acetate. Evaporation gave 1.1 gr of a light yellow oil, 54percent yield, which on standing crystallized. mp- 85. [NMR CDC13] 7.20 (4H, AB q, J=8. [6 HZ),] 3.50 (2H, m) 3.20 [(1 H,] m), 2.81 (2H, m). NMR tyrosine ethyl ester free base [CDCI3] 7.0, 6.56 (4H, AB q, J=8.8 Hz), 4.20 (2H, q, J=7,0 Hz), 3. [70,] 3.0, 2.80 (3H, 12 line ABXm), 1.28. (3H, t, J=7.0 Hz). JACS, 71,305 (1949). Biels.-E3, Vol. 13, p 2263.
54% With lithium aluminium tetrahydride; In diethyl ether; at 20℃; for 3h; Synthesis b: Compound b (tyrosinol) To 3 g, 12 mM, L-tyrosine ethyl ester HCl in 50 ml dry ether was added 1.2 g 32 mM LiAlH4. After stirring 3 hours at room temperature, water and KOH were added and the reaction was extracted with ethyl acetate. Evaporation gave 1.1 g of a light yellow oil, 54percent yield, which on standing crystallized. mp-85. NMR CDCl3 7.20 (4H, AB q, J=8.6 Hz), 3.50 (2H, m) 3.20 (1H, m), 2.81 (2H, m). NMR tyrosine ethyl ester free base CDCl3 7.0, 6.56 (4H, AB q, J=8.8 Hz), 4.20 (2H, q, J=7.0 Hz), 3.70, 3.0, 2.80 (3H, 12 line ABXm), 1.28. (3H, t, J=7.0 Hz). JACS 71, 305(1949). Biels, E3, Vol. 13, p 2263.
54% With lithium aluminium tetrahydride; In diethyl ether; at 20℃; for 3h; To 3g 12 mM, L-tyrosine ethyl esterHCl in 50 ml dry ether was added 1.2g 32 mM LiAlH4. After stirring 3 hours at room temperature, water and KOH were added and the reaction was extracted with ethyl acetate. Evaporation gave l. l g of a light yellow oil, 54percent yield, which on standing crystallized. mp-85. NMR CDCl3 7.20 (4H, AB q, J=8.6 Hz), 3.50 (2H, m) 3.20 (lH, m), 2.81 (2H, m). NMR tyrosine ethyl ester free base CDCl3 7.0, 6.56 (4H, AB q, J=8. 8 Hz), 4.20 (2H, q, J=7,0 Hz), 3.70, 3.0, 2.80 (3H, 12 line ABXm), 1. 28. (3H, t, J=7.0 Hz).
 

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